메뉴 건너뛰기




Volumn 354, Issue 18, 2012, Pages 3545-3550

[3+2]Cycloaddition of propargylamines and α-acylketene dithioacetals: A synthetic strategy for highly substituted pyrroles

Author keywords

acylketene dithioacetals; 3+2 cycloaddition; propargylamines; pyrroles; synthetic methods

Indexed keywords


EID: 84871088337     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201200375     Document Type: Article
Times cited : (26)

References (63)
  • 1
    • 84871072236 scopus 로고    scopus 로고
    • For reviews, see
    • For reviews, see
  • 5
    • 84871076736 scopus 로고    scopus 로고
    • For selected recent reports, see
    • For selected recent reports, see
  • 22
    • 84871081621 scopus 로고    scopus 로고
    • For a 4-step synthesis of polysubstituted pyrroles via N-propargyl β-enaminone intermediate, see
    • For a 4-step synthesis of polysubstituted pyrroles via N-propargyl β-enaminone intermediate, see
  • 23
    • 60949109743 scopus 로고    scopus 로고
    • For a review on addition of metal enolate derivatives to unactivated carbon carbon multiple bonds, see
    • S. Cacchi, G. Fabrizi, E. Filisti, Org. Lett. 2008, 10, 2629. For a review on addition of metal enolate derivatives to unactivated carbon carbon multiple bonds, see
    • (2008) Org. Lett. , vol.10 , pp. 2629
    • Cacchi, S.1    Fabrizi, G.2    Filisti, E.3
  • 25
    • 84871078280 scopus 로고    scopus 로고
    • For reviews, see
    • For reviews, see
  • 32
    • 43949131442 scopus 로고    scopus 로고
    • (Barton-Zard pyrrole synthesis: cyclization between a nitroalkene and isocyanoacetate)
    • N. Ono, Heterocycles 2008, 75, 243 (Barton-Zard pyrrole synthesis: cyclization between a nitroalkene and isocyanoacetate)
    • (2008) Heterocycles , vol.75 , pp. 243
    • Ono, N.1
  • 33
    • 0000243566 scopus 로고    scopus 로고
    • (Van Leusen pyrrole synthesis: cyclization between a Michael acceptor and tosylmethyl isocyanide).
    • D. Van Leusen, A. M. van Leusen, Org. React. 2001, 57, 417 (Van Leusen pyrrole synthesis: cyclization between a Michael acceptor and tosylmethyl isocyanide).
    • (2001) Org. React. , vol.57 , pp. 417
    • Van Leusen, D.1    Van Leusen, A.M.2
  • 34
    • 84871082937 scopus 로고    scopus 로고
    • For selected recent reports on pyrrole synthesis relying on alkynes, see
    • For selected recent reports on pyrrole synthesis relying on alkynes, see
  • 52
    • 33646236946 scopus 로고    scopus 로고
    • For a review on the synthesis of methylenepyrrolidines by formal [3+2] cycloadditions of propargyl substrates, see
    • S. Morikawa, S. Yamazaki, Y. Furusaki, N. Amano, K. Zenke, K. Kakiuchi, J. Org. Chem. 2006, 71, 3540. For a review on the synthesis of methylenepyrrolidines by formal [3+2] cycloadditions of propargyl substrates, see
    • (2006) J. Org. Chem. , vol.71 , pp. 3540
    • Morikawa, S.1    Yamazaki, S.2    Furusaki, Y.3    Amano, N.4    Zenke, K.5    Kakiuchi, K.6
  • 56
    • 84871064058 scopus 로고    scopus 로고
    • Commencial 3-phenylprop-2-yn-1-aminium chloride (3b) was used directly as the amine component.
    • Commencial 3-phenylprop-2-yn-1-aminium chloride (3b) was used directly as the amine component.
  • 57
    • 79959464695 scopus 로고    scopus 로고
    • 3-[Ethylthio(aryl)methylene]pentane-2,4-diones 9 were synthesized by Cu-catalyzed desulfitative C-C bond-forming reaction of 1a with arylboronic acids, see.
    • 3-[Ethylthio(aryl)methylene]pentane-2,4-diones 9 were synthesized by Cu-catalyzed desulfitative C-C bond-forming reaction of 1a with arylboronic acids, see:, Y. Dong, M. Wang, J. Liu, W. Ma, Q. Liu, Chem. Commun. 2011, 47, 7380.
    • (2011) Chem. Commun. , vol.47 , pp. 7380
    • Dong, Y.1    Wang, M.2    Liu, J.3    Ma, W.4    Liu, Q.5
  • 58
    • 84871077720 scopus 로고    scopus 로고
    • CCDC 854945 (10a) contains the supplementary crystallographic data for this paper. Thes data can be obtained free of charge via
    • CCDC 854945 (10a) contains the supplementary crystallographic data for this paper. Thes data can be obtained free of charge via www.ccdc.cam.ac.uk/ data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.